Team:Frankfurt/Notebook

From 2012.igem.org

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You should make use of the calendar feature on the wiki and start a lab notebook.  This may be looked at by the judges to see how your work progressed throughout the summer.  It is a very useful organizational tool as well.
You should make use of the calendar feature on the wiki and start a lab notebook.  This may be looked at by the judges to see how your work progressed throughout the summer.  It is a very useful organizational tool as well.
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==Methods and Protocols==
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=Methods and Protocols=
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=Culture Medium=
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==Culture Medium==
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pH has to be regulated with NaOH to pH=7.5
pH has to be regulated with NaOH to pH=7.5
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<br>
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<br> <br>
Every cluture medium has to be autoclaved.
Every cluture medium has to be autoclaved.
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==Agar Plate==
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=Agar Plate=
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===LB<sup>ampicillin</sub>-Agar===
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Add 2 % agar to LB-medium. After autoclaving and cooling-down to 60 °C steril ampicillin is added. Plates were poured.
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===SCD-Agar===
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Add 2 % agar to SCD-medium. After autoclaving and cooling-down steril amino acid solution is added. Dependent on the respective selective medium Histidin (0.25 mM), Trypthophan (0.19 mM), Uracil (0.44 mM) or Leucin (0.35 mM) is added.
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===YEPD-Agar===
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Add 2 % agar to YEPD-medium

Revision as of 14:32, 14 September 2012

Frankfurt logo.png
Home Team Project Organisms New Yeast RFC Notebook Registered Parts Modeling Safety Attributions Official Team Profile

You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well.

Contents

Methods and Protocols

Culture Medium

Full Medium (YEPD) for Yeast
Yeast Extract1 % (weight/volume)
Pepton2 % (w/v)
Glucose2 % (w/v)
Synthetic Complete Medium (SC) for Yeast
Yeast Nitrogen Base0.17 % (w/v)
Ammoniumsulfate0.5 % (w/v)
Amino Acid Mix*50 ml/l
Histidin**0.25 mM
Tryptophan**0.19 mM
Leucin**0.35 mM
Uracil**0.44 mM

pH has to be regulated with KOH to pH=6.3
!* contains no His, Leu, Trp and Uracil
** addition of this components depents on the respective selection medium

SOC-Medium for Regeneration of transformed Escherichia coli`s after Electroporation
Trypton2 % (w/v)
Yeast Extract0.5 % (w/v)
NaCl10 mM
KCl2,5 mM
MgCl210 mM
MgSO410 mM
Glucose20 mM

pH has to be regulated to pH=6.8-7.0

Full Medium (YEPD) for Yeast
Yeast Extract1 % (weight/volume)
Trypton0.5 % (w/v)
NaCl0.5 % (w/v)

pH has to be regulated with NaOH to pH=7.5

Every cluture medium has to be autoclaved.

Agar Plate

LBampicillin</sub>-Agar

Add 2 % agar to LB-medium. After autoclaving and cooling-down to 60 °C steril ampicillin is added. Plates were poured.

SCD-Agar

Add 2 % agar to SCD-medium. After autoclaving and cooling-down steril amino acid solution is added. Dependent on the respective selective medium Histidin (0.25 mM), Trypthophan (0.19 mM), Uracil (0.44 mM) or Leucin (0.35 mM) is added.

YEPD-Agar

Add 2 % agar to YEPD-medium